Synthesis of Compounds with Juvenile Hormone Activity, XXVII. Synthesis of Enantiomerically Pure (10R,11S)‐(+)‐Juvenile Hormone 0
- 17 January 1989
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1989 (1) , 41-44
- https://doi.org/10.1002/jlac.198919890109
Abstract
The synthesis of (10R,11S)‐(+)‐juvenile hormone 0 (1) was achieved by employing an improved method for the construction of a trisubstituted double bond.Keywords
This publication has 9 references indexed in Scilit:
- Synthesis of enantiomerically pure (10,11)-(+)-juvenile hormones I and IITetrahedron, 1988
- JH Zero: New Naturally Occurring Insect Juvenile Hormone from Developing Embryos of the Tobacco HornwormScience, 1980
- Stereoselective synthesis of β-substituted α,β-unsaturated esters by dialkylcuprate coupling to the enol phosphate of β-keto estersCanadian Journal of Chemistry, 1979
- THE STEREOSELECTIVE SYNTHESIS OF C18-JUVENILE HORMONE ANALOGUEChemistry Letters, 1975
- Stereoselective addition of organocopper reagents to acetylenic esters and amides. Synthesis of juvenile hormone analogsJournal of the American Chemical Society, 1975
- THE STEREOSPECIFIC PREPARATION OF METHYL FARNESOATE AND SYNTHETIC PRECURSORS OF C18- AND C17 JUVENILE HORMONESChemistry Letters, 1974
- THE HIGHLY STEREOSELECTIVE SYNTHESIS OF ETHYL GERANATEChemistry Letters, 1974
- A New General Synthesis of Isoprenoid Chains Employing the Reaction of Dialkylcuprates with β-Acetoxy α,β-Unsaturated EstersSynthetic Communications, 1973
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973